{{Rsnum
|rsid=1012729
|Gene=WNK1
|Chromosome=12
|position=878316
|Orientation=plus
|ReferenceAllele=G
|GMAF=0.2865
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=WNK1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 50.4 | 39.8 | 9.7
| HCB | 63.5 | 31.4 | 5.1
| JPT | 61.1 | 37.2 | 1.8
| YRI | 24.5 | 50.3 | 25.2
| ASW | 29.8 | 50.9 | 19.3
| CHB | 63.5 | 31.4 | 5.1
| CHD | 59.6 | 35.8 | 4.6
| GIH | 41.6 | 42.6 | 15.8
| LWK | 33.0 | 46.8 | 20.2
| MEX | 48.3 | 44.8 | 6.9
| MKK | 41.7 | 45.5 | 12.8
| TSI | 53.9 | 40.2 | 5.9
| HapMapRevision=28
}}
[[rs1012729]] is a SNP in the WNK lysine deficient protein kinase 1 [[WNK1]] gene.

In the Avon Longitudinal Study of Parent and Children Study (5326 subjects measured for systolic blood pressure at 11 years of age), [[rs1012729]](G) carriers were associated with a gender-adjusted change in a diastolic [[blood pressure]] gradient of -0.11 mm Hg/y (CI: -0.20 to -0.03 mm Hg/y; p=0.0054). This variant also showed association with systolic [[blood pressure]]. {{PMID|18809789}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}